| Tag | Content |
|---|
EnhancerAtlas ID | HS095-32616 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chrX:134137740-134138840 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chrX:134138309-134138324 | CAGGCCACGCCCATG | + | 6.1 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH0XI135003 | chrX | 134137631 | 134138935 |
| Enhancer Sequence | TCCTAATATA GCAAATTAAT AGATTTCTGA ACATTTAACC CACCTTCTAT TAACTGTTCA 60
TGGTGCATTA CTCTTTGAAT GTGCTGCTCT GGATGTTTGC TAATATTTGG GGCTTTCCTA 120
TTAATGTTTC AAAGTAACCA CATCTGCGGC CAGGGAGCCA ATAATCTGGC TGAGAGATGC 180
ATGAAGGAGG AAAATGTGTT CACAGAACCT CACTCCAGTG GCGTCCACAG CCGAGAGTCA 240
GTAAAGGGAC ACGCTACAGC TGATGAGTTA GGTGAGGGGA GGAGTACGGT AGGAGGCCGC 300
ATCACCTTCC AGAACACGTG TCCTCTGCTC TCTTTGGGCA GCGGGCGCAA TCTCCCCTCA 360
CACCGCAAAC TGTCCTGGGA TCTTCCCCCG CGCACCGCCC CTCGCCCGCG CCTGCCTTGG 420
GAAATCTTGG CCCCACCTTT CTGATTCAGA CCCCGCCTCC TGAAGAGAGT TAAGCCCTCC 480
CCCACGTTCT CACAGCCGCG GCCCGGCCCC GTTCTGAGCT TGCGCACTAG TGACCATCGG 540
GCTTTGGGGG CGGAGCCCGC GCAAGCACTC AGGCCACGCC CATGGCCAAG CCCACATTCC 600
GCCCCATGGA CAGGCCCACA TTCCGCCCCA TGGACACGCC TCCACAACCA TGCATTTCCG 660
GTGATGCTTA GAAATATAAA GATCGGAGTG GTAATGTAAT TTTGTGACGT TGGTGAAAGA 720
CTAAAAGCAA ATGGCAAAAT CATACCCACT GACCTGAAAT AGGGTCCAAA TCGGGACAAA 780
AAGGACATTT TTCTTTGCCT CCACCCTCTG ACACAGCCTT TAGGAGGACA ATGCCCTACG 840
GCTGCCCCCA GCTGCCTAGA ATCCACTCTA CCCCAGACTA CAGTGACAAT TCTAAGCCCA 900
CCTGTCTTAT GCAGAAACCG GGAGGCAGAA GGGGGCACAC AACAGGAAGG GGAAGAAATG 960
TTCTCTGAGG GAGAAACAGG TCCGTTTGGC ACTTTCCACA GATGCACCCA ACTCCGACTG 1020
GAATAACTGC TGCTTACTCC TCTGCTCATT GTGTCTTTGC AATTAAAAGA AAAAATTGAA 1080
GTAATTATCT CTGGTGAGTC 1100
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